Mellitic acid

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Mellitic acid[1]
Skeletal formula
Ball-and-stick model
Space-filling model
Names
Preferred IUPAC name
Benzenehexacarboxylic acid
Other names
Graphitic acid
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
DrugBank
ECHA InfoCard 100.007.495 Edit this at Wikidata
UNII
Properties
C12H6O12
Molar mass 342.16 g/mol
Density 1.68 g/cm3, 2.078 (calc.)[2]
Melting point > 300 °C (572 °F; 573 K)
Boiling point 678 °C (1,252 °F; 951 K) (calc.)[2]
Acidity (pKa) 1.40, 2.19, 3.31, 4.78, 5.89, 6.96[3]
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

Mellitic acid, also called graphitic acid or benzenehexacarboxylic acid, is an acid first discovered in 1799 by Martin Heinrich Klaproth in the mineral mellite (honeystone), which is the aluminium salt of the acid.[4] It crystallizes in fine silky needles and is soluble in water and alcohol.

Preparation[]

Mellitic acid may be prepared by warming mellite with ammonium carbonate, boiling off the excess of the ammonium salt, and adding ammonia to the solution. The precipitated alumina is filtered off, the filtrate evaporated, and the ammonium salt of the acid purified by recrystallization. The ammonium salt is then converted into the lead salt by precipitation with lead acetate, and the lead salt is then decomposed by hydrogen sulfide. The acid may also be prepared by the oxidation of pure carbon, graphite or hexamethylbenzene, by alkaline potassium permanganate in the cold, or by hot concentrated nitric acid.[5]

Reactions[]

It is a very stable compound; chlorine, concentrated nitric acid and hydriodic acid do not react with it. It is decomposed, on dry distillation, into carbon dioxide and , C10H6O8; when distilled with lime it gives carbon dioxide and benzene. Long digestion of the acid with an excess of phosphorus pentachloride forms the acid chloride, which crystallizes in needles, and melts at 190 °C. By heating the ammonium salt of the acid to 150–160 °C while ammonia is evolved, a mixture of paramide (mellimide, molecular formula C
6(CONHCO)
3), and is obtained. The mixture may be separated by dissolving out the ammonium euchroate with water. Paramide is a white amorphous powder, insoluble in water and alcohol.

The high stability of mellitic acid salts and their presence as an endproduct of the oxidation of polycyclic aromatic hydrocarbons, which are present in the solar system, make them a possible organic substance in Martian soil.[6]

Mellitates (and salts of other ) of iron and cobalt have interesting magnetic properties.[7]

See also[]

References[]

  1. ^ MSDS for mellitic acid[permanent dead link]
  2. ^ Jump up to: a b Curate Data: Predicted Properties: 2244. ChemSpider.com.
  3. ^ Brown, H.C., et al., in Baude, E.A. and Nachod, F.C., Determination of Organic Structures by Physical Methods, Academic Press, New York, 1955.
  4. ^ Klaproth (1802). Beiträge zur chemischen Kenntniss der Mineralkörper, Band 3 (in German). p. 114.
  5. ^ WebElements.com
  6. ^ S. A. Benner; K. G. Devine; L. N. Matveeva; D. H. Powell (2000). "The missing organic molecules on Mars". Proceedings of the National Academy of Sciences. 97 (6): 2425–2430. doi:10.1073/pnas.040539497. PMC 15945. PMID 10706606.
  7. ^ Kurmoo M, Estournes C, Oka Y, Kumagai H, Inoue K (2005) Inorganic Chemistry volume 44, page 217

Further reading[]

Henry Enfield Roscoe, Carl Scholemmer, "Mellitene Group", "A Treatise on Chemistry: V.III: The Chemistry of the Hydrocarbons and their Derivatives on Organic Chemistry: P.V:529. D. Appleton and Co. (1889).

 This article incorporates text from a publication now in the public domain: Chisholm, Hugh, ed. (1911). "Mellitic Acid". Encyclopædia Britannica. 18 (11th ed.). Cambridge University Press. p. 95.

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